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iTRAQ 标记二维液相色谱-串联质谱分析去神经支配大鼠比目鱼肌差异表达蛋白。

iTRAQ-coupled 2D LC-MS/MS analysis on differentially expressed proteins in denervated tibialis anterior muscle of Rattus norvegicus.

机构信息

Jiangsu Key Laboratory of Neuroregeneration, Nantong University, 19 Qixiu Road, Nantong 226001, Jiangsu Province, China.

出版信息

Mol Cell Biochem. 2012 May;364(1-2):193-207. doi: 10.1007/s11010-011-1218-2. Epub 2012 Jan 7.

Abstract

To understand the molecular aspects of denervation-induced atrophy of skeletal muscles, isobaric tags for relative and absolute quantitation (iTRAQ) coupled with two-dimensional liquid chromatography-tandem mass spectrometry were performed to detect a total of 260 proteins that were differentially expressed in the rat tibialis anterior muscle at different times (1, 4, and 8 weeks) after rat sciatic nerve transection. Western blot, gene ontology, and Kyoto Encyclopedia of Genes and Genomes analyses were further conducted for protein validation, functional annotation, and pathway identification, respectively. Among 260 dysregulated proteins, metabolic enzymes represented the largest class of proteins differentially expressed; a down-regulation of β-enolase might be associated with a decreased expression of fast-twitch myosin-4; the 14-3-3 proteins displayed an up-regulation, which might facilitate the inhibition of mTOR signaling; an up-regulation of α-crystallin B chain might be related to the later onset and the slower progress of atrophy; an up-regulation of phosphatidylethanolamine-binding protein-1 perhaps progressively abrogated the cell survival and antiapoptotic properties during muscle atrophy. These results might contribute to the understanding of molecular mechanisms regulating denervation-induced muscle atrophy.

摘要

为了理解失神经支配诱导的骨骼肌萎缩的分子机制,采用等重同位素标记相对和绝对定量技术(iTRAQ)结合二维液相色谱-串联质谱技术,检测到大鼠坐骨神经横断后不同时间(1、4 和 8 周)大鼠比目鱼肌中差异表达的总共 260 种蛋白质。进一步进行 Western blot、基因本体论和京都基因与基因组百科全书分析,分别用于蛋白质验证、功能注释和途径鉴定。在 260 种失调蛋白中,代谢酶代表差异表达蛋白中最大的一类;β-烯醇酶的下调可能与快肌肌球蛋白-4表达降低有关;14-3-3 蛋白呈上调表达,可能有助于抑制 mTOR 信号;α-晶体蛋白 B 链的上调可能与萎缩的后期发生和进展较慢有关;磷酸乙醇胺结合蛋白-1 的上调可能逐渐破坏肌肉萎缩过程中的细胞存活和抗凋亡特性。这些结果可能有助于理解调节失神经支配诱导的肌肉萎缩的分子机制。

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